نتائج البحث

Mutant TDP-43 does not impair mitochondrial bioenergetics in vitro and in vivo.

• Authors : Hibiki Kawamata¹; Peixoto, Pablo²; Konrad, Csaba¹

• Source: Molecular Neurodegeneration. 5/8/2017, Vol. 12, p1-15. 15p. 1 Black and White Photograph, 2 Charts, 4 Graphs.

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Stathmin 1/2-triggered microtubule loss mediates Golgi fragmentation in mutant SOD1 motor neurons.

• Authors : Bellouze, Sarah¹; Baillat, Gilbert¹; Buttigieg, Dorothée¹

• Source: Molecular Neurodegeneration. 6/9/2016, Vol. 11, p1-20. 20p. 2 Charts, 6 Graphs.

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Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling.

• Authors : Alemasov, Nikolay A.¹ ; Ivanisenko, Nikita V.^1,2; Ramachandran, Srinivasan^3,4

• Source: BMC Structural Biology. 2/5/2018, Vol. 18, p1-1. 1p. 1 Diagram, 4 Charts, 6 Graphs.

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Comparative analysis of the time-dependent functional and molecular changes in spinal cord degeneration induced by the G93A SOD1 gene mutation and by mechanical compression

• Authors : Malaspina, A; Jokic, N; Huang, WL

Subjects: AMYOTROPHIC-LATERAL-SCLEROSIS; DIFFERENTIAL EXPRESSION; ACTIVATED MACROPHAGES

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Correction to: selected articles from Belyaev Conference 2017: structural biology

• Authors : Orlov, Yuriy L; Baranova, Ancha V

Subjects: Evolution, Molecular; Models, Molecular; Superoxide Dismutase-1

• Source: BMC Structural Biology

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